A polyolefin composition having an increased modulus of elasticity as well as increased heat resistance, wherein the polymer composition has high melt viscosity, and wherein the composition contains a carbon material as a filler, wherein the filler is present in the form of a carbon nanofiber.

Patent
   8859670
Priority
May 25 2009
Filed
May 20 2010
Issued
Oct 14 2014
Expiry
Jan 06 2031
Extension
231 days
Assg.orig
Entity
Large
1
17
currently ok
1. A polymer composition having an elasticity modulus increased relative to that of the pure polymer matrix, with a simultaneously increased heat distortion resistance, notched impact strength, retention or improvement in the profile of the chemical stability, and a reduction in the creep tendency, the polymer composition comprising as filler a carbon material, wherein the filler is present in the form of a nanofiller comprising carbon nanofibers homogeneously distributed in the polymer matrix, wherein the polymer composition comprises a polyolefin having a melt index of less than 2 g/10 min in accordance with method 190/5 to ISO 1133, wherein the carbon nanofibers are not chemically surface-modified.
6. A process for preparing a polymer composition having an elasticity modulus increased relative to that of the pure polymer matrix, with a simultaneously increased heat distortion resistance, notched impact strength, retention or improvement in the profile of the chemical stability, and a reduction in the creep tendency, the polymer composition comprising as filler a carbon material, wherein the filler is present in the form of a nanofiller comprising carbon nanofibers homogeneously distributed in the polymer matrix, wherein the polymer composition comprises a polyolefin having a melt index of less than 2 g/10 min in accordance with method 190/5 to ISO 1133, the process comprising the steps of introducing the carbon nanofibers and homogeneously distributing the carbon nanofibers in the polymer matrix by direct compounding or masterbatch in a pure polymer matrix, wherein the compounding is carried out without compatibilizers, wherein the carbon nanofibers are not chemically surface-modified.
2. The polymer composition as claimed in claim 1, wherein the polymer is a high-density polyethylene.
3. The polymer composition as claimed in claim 2, wherein the polymer is a crosslinked polyethylene.
4. The polymer composition as claimed in claim 1, wherein the polymer is a polypropylene.
5. The polymer composition as claimed in claim 1, wherein the carbon nanofiber filler has a weight fraction of less than 30% by weight.
7. The process as claimed in claim 6, including forming the polymer composition by conventional extrusion into industrial pipeline construction or plant construction for the transport of aggressive gaseous or liquid media.
8. The process as claimed in claim 6, including forming the polymer composition by conventional extrusion to give pipes, plates or rods or by injection molding to give injection moldings.
9. The polymer composition as claimed in claim 1, wherein the polymer composition includes conventional additives for increasing the thermal conductivity.
10. The process as claimed in claim 6, including forming the polymer composition into heat exchangers.

The invention relates to a polymer composition having an elasticity modulus increased relative to that of the pure polymer matrix, with a simultaneously increased heat distortion resistance, notched impact strength, retention or improvement in the profile of the chemical stability, and a reduction in the creep tendency, the polymer composition comprising as filler a carbon material.

In pipeline construction, pipelines made of polyolefins and polyolefin compositions are used. For the most common areas of application, polyethylene, polypropylene, polybutylene and polyvinyl chloride compositions are adequately available on the market. Enhanced materials with a higher elasticity modulus and a simultaneously increased heat distortion resistance, which can be used in specialty areas of application such as the transport of aggressive media, are not available at affordable prices. The focal points in the development of new plastics compositions lie in the areas of coextrusion, functional coating, drawing, and thermoset/fiber composites. The development programs of the raw materials manufacturers take no account primarily of affordable plastics compositions suitable for the extrusion of pipelines.

The improvement in the profiles of properties of the raw materials used in plastics pipeline construction has seen no significant further advance in recent years. As far as we are aware, innovations have been primarily in the area of enhancements through extrusion, functional coating, biaxial drawing or reinforcement by thermoset/fiber composites.

In the industrial pipe segment, the name manufacturers, with regard to polyolefins (PE, PP, PB), have already achieved, on the raw materials side, a comparable high quality level, with the consequence that market promotion is increasingly coming down to a pure price proposition. In many applications, a similar development can be seen in the area of PVC materials.

In the plastics industrial pipe segment, the desire of the users for significant—but also affordable—improvements in materials is known. As a result of the comparatively small size of this segment, however, this desire has not met sufficient priority on the part of the raw materials manufacturers for a number of years.

Known systems are the reinforcement of plastics by means of fillers→C fillers→C-based nanofillers, published in US 2006 0001013A1, WO 2008/041965 A2 or WO 2009/000408 A1.

Furthermore, the dispersion problems of C-based fillers and nanofillers are described in WO 2009/000408 A1.

Only through homogeneous dispersion is it possible for the nanofillers to develop their properties; conclusions are independent of the nature of the nanofillers.

The factors governing the dispersibility of a nanofiller include size, surface structure, chosen matrix, its molecular weight/melt viscosity, and the method of compounding that is selected (machine composition, number of stages, etc.). Furthermore, system-specific compatibility additives can be used, as described in U.S. Pat. No. 7,479,516 B2 or WO 29027357A1.

The system compatibilities of nanofillers with a selected polymer can usually not be simply transposed to other classes of polymer, but instead require individual adaptation. Even simply the lowering of the melt viscosity of the polymers from typical injection molding grades to extrusion grades raises entirely new issues with regard to the dispersion of nanofillers. Ways of dispersion described to date in patent literature for CNT/CNF are as follows: WO 29027357 A1, US 2009 0008 611, WO 2006096203 A2, EP 2028218 A1, US 2006 001013 A1 and WO 2008041965 A2.

The fundamental advantage of CNT/CNF reinforced polymers is known theoretically in the literature (good energy transport properties, improved mechanical properties, with lower degrees of filling as compared with conventional carbon black filling).

The consequences of the reinforcement of polymers matrices with C-based nanofillers for the chemical stability profile of the material have so far not been described in the literature.

Fundamental attractiveness of the carbon nanofiller approach for polymers for industrial plant construction/pipeline construction. Expectations:

The objective of the invention is

The key challenges for the invention are the retention of or improvement in the pressure resistance (MRS class), the significant (as far as possible >30%) increase of stiffness and impact strength (particularly for PP), the thermal conductivity, the retention of the relative improvement when the service temperature is raised, the improvement of the chemical stability, and the additional benefit, an example being the reduction in thermal expansion and/or the improvement in energy transport properties.

EP 2 028 218 A1 discloses a polymer composition which besides polyolefins and polyhydroxycarboxylic acid as copolymer further comprises carbon nanotubes. The polymer composition may be used, for example, in heat exchangers, where good thermal conductivity is required. The electrical conductivity can be improved as well. Because the carbon nanotubes tend toward agglomeration, homogeneous mixing of the new composition is difficult to achieve. As a consequence of this, mechanical weak points in the end product cannot be ruled out. The polymer matrix is prepared using a metallocene catalyst. The melt viscosity or MFI (melt flow index) of the polymer composition is so unfavorable that pipes or plastic moldings cannot be produced economically by the injection molding process.

Starting from this prior art, it is an object of the invention to specify a polymer composition which is easy to prepare and which, with production costs that are as low as possible, exhibits mechanical properties that are as good as possible, and which can be processed in the injection molding process. Achievement of this object will also allow a plastics material to be offered that is suitable for aggressive media.

The foregoing object is achieved by the filler being present in the form of a nanofiller, more particularly in the form of carbon nanofibers.

The polymer composition may be a polyolefin having a melt index of less than 2 g/10 min in accordance with method 190/5 to ISO 1133.

Preferred developments of the invention are apparent from the dependent claims.

The individual components are now described:

Polymer basis: Hostalen, PPH 2222 gray; MFR (190/5): 0.5 g/10 min.

Nanofillers:

CNT: Nanocyl 7000; Nanocyl SA.; MWCNT; no details of geometry; 90% C fraction; 10% metal oxide content; 250-300 g/m2 surface area

CNF: VGCF-H; Showa Denko, diameter: 150 nm: length=10-20 μm; aspect ratio˜100; 13 m2/g surface area; no information on purity

For the better dispersion of the MWNT and also in order to observe the necessary accuracy of the small proportions in the formulations, a masterbatch (90% Hostalen PP H2222+10% MWNT Nanocyl 7000) was compounded, and in subsequent extrusion steps was diluted to give the desired composition of the formulations.

The masterbatch was compounded using a closely intermeshing, co-rotating laboratory twin-screw extruder.

The system presented here thus describes for the first time the possibility of using commercially available CNF and a state-of-the-art compounding technology, along with a high-viscosity polyolefin material which is established in industrial plant construction, to produce a new composite material distinguished by the following properties:

Kretzschmar, Bernd, Schuessler, Stephan, Lendl, Michaela

Patent Priority Assignee Title
10550231, Mar 12 2015 Total Research & Technology Feluy Masterbatches for preparing a composite material based on semi-crystalline polymer with enhanced conductivity properties, process and composite materials produced therefrom
Patent Priority Assignee Title
5461096, Dec 31 1991 SABIC INNOVATIVE PLASTICS IP B V Polyphenylene ether resin-containing compositions containing high molecular weight polyethylene resin
7479516, May 22 2003 EVERMORE APPLIED MATERIALS CORP Nanocomposites and methods thereto
7938996, Oct 01 2004 Board of Regents, The University of Texas System Polymer-free carbon nanotube assemblies (fibers, ropes, ribbons, films)
8455583, Aug 02 2004 UNIVERSITY OF HOUSTON Carbon nanotube reinforced polymer nanocomposites
20040106719,
20060001013,
20080275177,
20090008611,
20090023851,
20090176911,
20100230131,
EP1349179,
EP2028218,
WO2006096203,
WO2008041965,
WO2009000408,
WO2009027357,
////
Executed onAssignorAssigneeConveyanceFrameReelDoc
May 20 2010Georg Fischer Rohrleitungssysteme AG(assignment on the face of the patent)
Oct 13 2011LENDL, MICHAELAGeorg Fischer Rohrleitungssysteme AGASSIGNMENT OF ASSIGNORS INTEREST SEE DOCUMENT FOR DETAILS 0272650598 pdf
Oct 18 2011KRETZSCHMAR, BERNDGeorg Fischer Rohrleitungssysteme AGASSIGNMENT OF ASSIGNORS INTEREST SEE DOCUMENT FOR DETAILS 0272650598 pdf
Oct 24 2011SCHUESSLER, STEPHANGeorg Fischer Rohrleitungssysteme AGASSIGNMENT OF ASSIGNORS INTEREST SEE DOCUMENT FOR DETAILS 0272650598 pdf
Date Maintenance Fee Events
Dec 17 2014ASPN: Payor Number Assigned.
Apr 02 2018M1551: Payment of Maintenance Fee, 4th Year, Large Entity.
Apr 06 2022M1552: Payment of Maintenance Fee, 8th Year, Large Entity.


Date Maintenance Schedule
Oct 14 20174 years fee payment window open
Apr 14 20186 months grace period start (w surcharge)
Oct 14 2018patent expiry (for year 4)
Oct 14 20202 years to revive unintentionally abandoned end. (for year 4)
Oct 14 20218 years fee payment window open
Apr 14 20226 months grace period start (w surcharge)
Oct 14 2022patent expiry (for year 8)
Oct 14 20242 years to revive unintentionally abandoned end. (for year 8)
Oct 14 202512 years fee payment window open
Apr 14 20266 months grace period start (w surcharge)
Oct 14 2026patent expiry (for year 12)
Oct 14 20282 years to revive unintentionally abandoned end. (for year 12)